LC580iMRecalls & reported problems
Pride Mobility Products Corp · An electric positioning chair is a device with a motorized positioning control that is intended for medical purposes and that can be adjusted to various positions. The device is used to provide stability for patients with athetosis (involuntary spasms) and to alter postural positions. · Class 2
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 3
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00606509400770), received between Apr 2, 2019 and May 10, 2021 — classified as 3 injuries, 1 malfunction.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.
Most reported problems
Device problems
- Appropriate Device Problem Term/Code Not Available4
Patient problems
- Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available1
- Bone Fracture(s)1
- Injury1
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
InjuryMay 10, 2021Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
ALLEGES THE BACK BROKE WHEN CONSUMER WAS IN THE PROCESS OF RAISING THE CHAIR TO GET OUT OF IT.
Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available
MAUDE report 11796069 ↗MalfunctionMar 18, 2020Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
PROVIDER ALLEGES CONSUMER GOT STUCK IN THE CHAIR IN THE MIDDLE OF THE NIGHT AND HAD TO CALL THE PARAMEDICS TO GET OUT OF THE CHAIR.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 9847452 ↗InjuryOct 29, 2019Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
CONSUMER'S DAUGHTER ALLEGES THE CHAIR WAS RECLINED NOT FULLY WITH ONE LEG STILL UP ON THE BACK OF THE CHAIR. SHE ALLEGES HER FATHER HAD SOME HOW FALLEN OUT OF THE SIDE OF THE CHAIR.
Patient problems: Bone Fracture(s)
MAUDE report 9249953 ↗InjuryApr 2, 2019Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
ALLEGES LEANING AGAINST THE CHAIR WHEN IT WAS IN AN UPRIGHT POSITION AND THE CHAIR AND CONSUMER FELL OVER.
Patient problems: Injury
MAUDE report 8473964 ↗
Other Chair, Positioning, Electric devices
- TruRize 3333Stryker Corporation · Chair, positioning, electric1 recall1 death53 reports
- EasyStand Bantam SmallAltimate Medical Inc. · Chair, Positioning, Electric1 recall0 reports
- EasyStand Bantam Extra SmallAltimate Medical Inc. · Chair, Positioning, Electric1 recall0 reports
- LC358XXL LC358XXL/CA358XXLPride Mobility Products Corp · Chair, Positioning, Electric21 reports
- LC358L LC358L/CA358LPride Mobility Products Corp · Chair, Positioning, Electric21 reports
- LC358XL LC358XL/CA358XLPride Mobility Products Corp · Chair, Positioning, Electric18 reports
- LC250Pride Mobility Products Corp · Chair, Positioning, Electric12 reports
- LC358M LC358M/BC358M/CA358MPride Mobility Products Corp · Chair, Positioning, Electric1 death11 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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